“January 14, 2010…a day that will live in infamy!  Well, okay, maybe that’s a bit of an exaggeration.  But it is certainly a date I am sure to never forget!  It’s the date I heard the surgeon inform me that the lump in my breast was malignant…cancer.  Few people are ever ready to hear that diagnosis; it never crossed my mind that it was even a remote possibility for me.

Most people close to me know that one of my goals is to live to be 105.  I even have a blog titled, ‘Thrive to 105’ (www.thriveto105.com).  I’ve always been remarkably healthy…no serious illnesses, no broken bones, no hospital stays except for my babies…and I’ve always prided myself on living a lifestyle that would afford me the longevity I’m looking for.  I love life, and living another 50+ years is something I look forward to with great anticipation!  So how could this be happening to me?

As my daughter sat with me in the first surgeon’s office where I was referred, he explained how they would cut into my breast, remove the lump, then perform the biopsy.  At that point, my question was would they do the biopsy while I was ‘under’ and, if it was malignant, remove whatever else they needed to remove?

The surgeon’s answer was, “No.  If it’s malignant, you have to come back for another surgery”.  Well, it didn’t make sense to me that I should have to go under the knife twice, so I opted to get a second opinion.  Little did I know this was the first small step on a journey I had never expected to take.

January was supposed to be an exciting time for me.  I was moving into my own new apartment after a divorce and many months not having a place to call my own!  As it turned out, my move date ended up to be two days after my biopsy.  Instead of deciding where to put things in my new place, I was worrying about how to deal with a potentially life-threatening disease.”

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So today I had a “treatment” that is commonly touched on when researching alternative therapies…one that is non-invasive (except for an IV needle) and one relatively easy to obtain without traveling to foreign countries or going to special clinics.  Today I received a High-Dose Vitamin C IV Treatment.

It’s not the first one I’ve done, so there wasn’t any apprehension on my part.  In fact, I was looking forward to it, as I generally am whenever I do treatments.  Attitude is of the utmost importance, you know…not just when fighting a cancer “battle”, but when fighting any chronic disease.

As I sat down in the barcalounger (nice and comfy) to get started, I had a headache.  By the end of my treatment, my headache was the least of my problems!  By the end of the treatment, I was feeling chilled, tired, and light-headed.  After getting a blanket from the nurse…I had to go to the bathroom (which always happens by the end of these treatments)!

Once I was up, I decided that getting warm by sitting in my convertible with the top down would be just as good as sitting under a blanket.  Although it did warm me up, by then I was fighting the urge to vomit (“No, God, please…not in the parking lot!!!”).  Fortunately, that didn’t happen…but I did have to go back into the office to use the bathroom again!

A trip to the post office and Target had been on my agenda after my treatment; but by this time, the only place my car was headed was home!  Thankfully, the caregiver who helps me care for my dad with dementia still had time on the clock.  After downing a glass of herbal ice tea, I made a b-line for my bedroom and a nap…that lasted for nearly two hours.  It was awesome!

When I got up, I couldn’t wait to eat and was craving a tuna sandwich.  But no tuna for me (mercury and mayonnaise…bad), so I had sole almondine, waffle fries (I know….not so good) and lightly steamed broccoli.  I was famished…and I was singing along with the music from the 70s music channel on the TV!  Back to normal!

I know that’s a rather long-winded way of getting to a point, but here it is:  My choice of therapy this day, although it made me feel sick for a few hours, left me feeling none the worse for wear when I awoke.  I dare say that the side effects of a treatment of chemotherapy would last far longer and would not normally (from what I understand) leave one with a hearty appetite!  In addition, nothing in the IV I had today compromised my immune system or destroyed any of my healthy cells.

I’m just sayin’….

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As 2012 is well underway, I am in the third year of my journey since being diagnosed with breast cancer on January 13, 2010.  It’s been an extremely enlightening and immensely challenging couple of years, to say the least.

For someone who loves to write…and especially loves to write in the first person…it’s been very interesting to me that I haven’t written more about this experience in my life.  I’ve yet to quite get a handle on why I haven’t, but I’m focused on changing that this year. I intended to create a blog site for posting about alternative cancer treatments, but setting up the blog site isn’t my forte’, if you will.  In lieu of that for now, I’ve decided to use this blog site to start sharing the vast amount of knowledge I’ve gained in two years in hopes of helping others who may be diagnosed or have loved ones who’ve been diagnosed with cancer.  Not only will the resources and information I write about give those interested in alternative therapies a road sign to follow, but it will also help any who choose the standard care treatments.  Much of what I will share can help with post-treatment lifestyle choices and ways to minimize the negative impact some of those treatments have.

My wish is that as people find out about and read my blog, they will pass it on.  I welcome questions or requests for help and/or further information and hope I can be a source of support and encouragement for others on their journeys!

Fighting with healthy alternatives!

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WOW…well over a month since I posted to my blog! I guess another apology is in order…this time for human error rather than technical difficulties! It’s kind of like the cobbler’s kid having no shoes; a writer never gets time to write her own “stuff” when she’s busy writing everyone else’s!

For those of you who don’t communicate with me personally on a daily or weekly basis, an update is in order. I’m not sure I had shared in my blog what “therapy” I had been doing very soon after my diagnosis, aside from drastically changing my eating habits, resting more, and lowering my stress. I had been following a protocol researched and discovered by a German doctor way back when, Dr. Budwig, who actually was nominated for seven Nobel Prizes for her research. She found that a mixture of flax seed oil and cottage cheese taken daily had a certain effect on the outer “shell” of cancer cells, which left them vulnerable and able to be destroyed by a healthy immune system.

It seemed easy enough, although I did resort to making it into a smoothie with frozen berries and some almond milk each morning. While I did that, I continued to read and research and found something that I found more interesting and (hopefully) a little more promising. It is a product called Protocel, which was developed decades ago and thwarted by the FDA and others over the years. So now it is sold online as simply a health supplement. It’s taken five times a day (which can be a bit challenging), and more than six hours cannot lapse between doses. The great thing about this “treatment” is that I can be a little more lax on my diet, i.e. I can eat a little meat, such as chicken. I can also have honey and pure maple syrup, and a moderate amount of whole grain carbs. The other stipulations have to do with avoiding certain supplements (high doses of Vitamin C and E, as well as COQ10, which I had been taking) and other alternative treatments.

In addition, I’m taking ellagic acid (raspberry seed extract) twice a day. This is one of the alternative treatments that doesn’t interfere with the effectiveness of the Protocel.

Without getting into any long explanations, Protocel literally attacks the cells themselves and “kills” them; and your body eliminates the dead cells through a process called “lysing”. This elimination can happen in many ways…runny nose, “crusty” eyes, daily body “functions”, etc. Tiredness in the first few weeks is about the only side effect. I’ll take that over hair loss, nausea, and the decimation of my immune system any day!

Oh yes, I also went to see an oncologist finally. It wasn’t a horrible visit overall, and I did learn a couple good facts regarding my biopsy that I hadn’t been told before. I learned my cells are estrogen receptive, which means estrogen feeds them, so I won’t be doing any bio-identical hormone replacement anytime soon. I also learned that they measure the “proliferation rate” of the cells and found 67% of mine were not prone to “proliferate” and only 23% were, which I think is pretty good odds. With what I’m doing right now, I’m thinking I can control that 23% and, in the end, get rid of all of them!

Of course, she encouraged me to do the standard of care treatment (chemo, surgery, radiation), to which I again said “NO!” In fact, if my memory serves me correctly, she told me they would first want me to do a short round of chemo BEFORE the surgery, which made absolutely no sense to me! Why do something that is going to destroy my immune system, then do surgery on diseased cells that will probably be released into my system elsewhere, into an immune system that has been compromised by previously ingested poison! It seems just so ludicrous! I was also asked what is in the Protocel. When I couldn’t tell her the ingredients, she told me I should at least know what was in it if I was going to be taking it. Later, reviewing the conversation at home, I thought, “I wouldn’t know what is in the chemotherapy drugs, but you’d expect me to take them!!!” At least I know I can take Protocel every day for years, and it won’t kill me!

So that’s my update! I’m feeling good, except for needing naps regularly; and I get kind of bored with my current meal plan. Much of that is my fault for being too lazy to prepare different recipes. It’s just easier to reach in and grab the organic greens/spinach, organic broccoli, bell pepper, celery, etc. and throw my homemade salad dressing on it! Bon appétit!

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I think part of my problem has to be brain overload.  I’m reading soooooooooooooooooooo much about treating cancer the natural way that some days I feel as though my head is going to explode!  It makes me obsessive at times now.  For instance…my lack of sleep…does not give my body the amount of time it needs to regenerate and get rejuvenated!  If I take naps later today, will that make up for at least part of my lack of sleep tonight?

Do people who are diagnosed with other life threatening diseases obsess over every little choice they make?  No sugar anymore…but is a tablespoon of honey in my green tea okay?  Limited carbs…but is my occasional whole grain baguette with my soup at Bread Co okay?  What if I eat an occasional homemade potato chip in a restaurant?  Am I eating enough “green stuff” each day?  Not eating meat…but damn…someone just told me shellfish are bad.  Alkaline water is preferable and so is organic everything!  No more regular milk or soy…almond milk, instead!  Thank God berries are highly recommended…but what if I can’t find organic ones???  Sheesh!

Of course, all the obsessing is definitely worth the outcome, which I’m feeling extremely positive about every day!  Besides, I can now fit into some capris that I haven’t worn in at least three or four years, so I guess I won’t complain too much!   LOL….

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That “revelation” should also be carried over to our internal “looks”.  We all (or most of us) start with the same parts:  heart, lungs, liver, brain, intestines, cells, etc.; however, the lives we lead soon make all of us so different on the inside.  Yet the traditional medical community wants to treat those of us diagnosed with cancer as identical!  They recommend a “standard of care” treatment that generally follows a daunting route…surgery, radiation, and chemotherapy.  In the traditional medical community, the faster they can get you under the knife and start introducing radiation and chemicals into your body, the faster they can “cure” you (or so they want you to believe).  Worse, if your cancer is in an advanced stage, they make the horrifying mistake of actually giving you a death sentence, turning off your brain to optimistic possibilities, and squashing what little hope you may be trying to cling to in order to get through treatment and RECOVER!!!

As I mentioned a couple of  weeks ago, I am doing a lot of reading about cancer…which I will be sharing in upcoming posts…but two of the most important things I’ve learned in the past two months are:

• People should be made aware that they have OPTIONS!  If someone (a surgeon or oncologist) tells you you have to have surgery, radiation, and/or chemotherapy, you need to understand that those are not your only options!  I’m not here to tell anyone what to do or that they should ignore the recommendations of their doctors…if they feel that is best for them and feel confident that the recommended treatment will make them better.  What I am saying is that you should “Take a deep breath” (which is what my very good friend, Linda, told me immediately after my diagnosis).  Do at least a little bit of research and reading, if only to find out how to make yourself the strongest you can be in order to come through surgery with the best odds of surviving without a recurrence or how to tolerate the chemicals you may be given.  YOU HAVE OPTIONS…AND IT’S IMPORTANT THAT YOU KNOW THIS!!

• No two people are alike.  Now, as you can tell from my story at the beginning of this post, I had already “discovered” this some time ago; but I’d never really considered it regarding my internal problems until my diagnosis.  NO TWO PEOPLE ARE ALIKE INTERNALLY, AND THIS SHOULD BE CONSIDERED WHEN TREATING CANCER. Although there are some things that all people who are diagnosed with cancer should do (which I will talk about at a later time), there are many things that should be assessed individually.  “Cookie cutter” treatment (surgery, radiation, chemotherapy) is not a good “standard of care”.

In upcoming posts, I will share a lot of what I’m learning in my attempt to “thrive to 105“!  I am confident that this little “blip on the radar screen” is not going to set me back or prevent me from getting there.  In fact, it may actually have been something I needed in order to assure I reach my goal!

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In their book called, Getting Well Again, Carl and Stephanie Simonton outline their research and an actual six-week program for helping those who are sick to use their minds as an aid to their healing process.  It’s a “step-by-step, self-help guide to overcoming cancer for patients and their families”.  Carl is an oncologist; Stephanie a psychiatrist…a powerful combination for the kind of work they’ve been doing for over three decades!

Part One of the book is titled:  The Mind and Cancer.  The first chapter is: The Mind-Body Connection; A Psychological Approach to Cancer Treatment.  It starts out dealing with the will to live, talks about the “whole-person approach” to treating cancer and discusses putting theory into practice.  My big takeaway from this chapter was:

It is our central premise that an illness is not purely a physical problem, but rather a problem of the whole person, that it includes not only body but mind and emotions.  We believe that emotional and mental states play a significant role both in susceptibility to disease, including cancer, and in recovery from all disease.  We believe that cancer is often an indication of problems elsewhere in an individual’s life, problems aggravated or compounded by a series of stresses six to eighteen months prior to the onset of cancer.  The cancer patient has typically responded to these problems and stresses with a deep sense of hopelessness, or “giving up”.  This emotional response, we believe, in turn triggers a set of physiological responses that suppress the body’s natural defenses and make it susceptible to producing abnormal cells.

WOW! As so many who are diagnosed with cancer must feel, I wondered “why” and “how” when I first heard the ‘c’ word.  But it made a lot of sense after reading the very detailed explanation in this book.  Eighteen months prior to my diagnosis (or possibly 24) I had the whole laundry list of events in my life that cause the most stress: I moved, I got married, I lost my job, my stepmom died, my relationships with the people I loved were strained, I got divorced.  At times I did feel a sense of hopelessness.  It makes so much more sense now.

Now understanding how the cells can become “abnormal”, it isn’t a hard segue to start wondering if it isn’t possible…with the right kind of physical and mental forces applied…to transform them into “normal” cells again.

We shall see!

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